Histiocytose.org - Histiocytose Langheransienne - histiocytose.org

L Association Histiocytose France. A pour but daider les personnes touchées par l histiocytose langerhansienne, une maladie rare et peu connue. Elle est ouverte à toutes les personnes atteintes ou concernées par la maladie. Le Groupe d Etude des Histiocytoses. Est une structure qui fédère des médecins impliqués à différents titres dans la prise en charge des patients enfants et adultes, ou dans la recherche biologique sur les histiocytoses.

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The web page histiocytose.org presently has an average traffic classification of zero (the smaller the superior). We have traversed two pages inside the website histiocytose.org and found eighteen websites associating themselves with histiocytose.org. There are two contacts and locations for histiocytose.org to help you communicate with them. The web page histiocytose.org has been online for one thousand one hundred and fifty-two weeks, eighteen hours, five minutes, and twenty-one seconds.
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HISTIOCYTOSE.ORG HISTORY

The web page histiocytose.org was first recorded on May 21, 2003. As of today, it is one thousand one hundred and fifty-two weeks, eighteen hours, five minutes, and twenty-one seconds young.
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LINKS TO WEBSITE

EHN International Network of Experts for Histiocytoses

Information for physicians, scientists, and other health professionals. Information for patients, families, and the interested public. Find experts for the different histiocytic diseases, all over the world. Understand why it is difficult to define expertise and how that problem is solved for this web portal. Raquo; Histio Net Newsletter.

LCH v.z.w. - De officiële belgische website van de Langerhans Cel Histiocytose

U kunt steunend lid worden vanaf slechts 15 euro per jaar. Maar ook losse giften zijn van harte welkom! U kan steunen door een storting op de rekening IBAN BE30 7343 7717 5011 van de vzw LCH Belgium. U krijgt minstens 1x per jaar een nieuwsbrief toegezonden, zodat u zelf kan zien wat uw bijdrage voor ons betekent heeft. Via onderstaand invulformulier kan u zich alvast lid maken. De middelen van de ve.

CENTRE MALADIES RARE COCHIN

ATELIERS FRANCOPHONES DE LA SCLERODERMIE. Vous y trouverez des i.

Accueil - Swiss group for Interstitial and Orphan Lung Diseases

Les pneumopathies interstitielles et maladies pulmonaires rares nécessitent une approche en réseau multidisciplinaire. Articles sur les maladies pulmonaires rares.

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CONTACTS

Association Histiocytose France

Association Histiocytose France

BP 60740

Melun Cedex, 77017

FR

Association Histiocytose France

Lydia DEBAR

41 rue grande

Blandy-le-Tours, 77115

FR

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Histiocytose.org - Histiocytose Langheransienne - histiocytose.org

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L Association Histiocytose France. A pour but daider les personnes touchées par l histiocytose langerhansienne, une maladie rare et peu connue. Elle est ouverte à toutes les personnes atteintes ou concernées par la maladie. Le Groupe d Etude des Histiocytoses. Est une structure qui fédère des médecins impliqués à différents titres dans la prise en charge des patients enfants et adultes, ou dans la recherche biologique sur les histiocytoses.

PARSED CONTENT

The web page states the following, "A pour but daider les personnes touchées par l histiocytose langerhansienne, une maladie rare et peu connue." I saw that the web page also stated " Elle est ouverte à toutes les personnes atteintes ou concernées par la maladie." They also said " Le Groupe d Etude des Histiocytoses. Est une structure qui fédère des médecins impliqués à différents titres dans la prise en charge des patients enfants et adultes, ou dans la recherche biologique sur les histiocytoses."

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